HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823917Generated: October 30, 2026
1-(Chloromethoxy)-2-methoxyethane → HCID 22147941, compound
https://huagongshe.com/reaction/1823917
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Chloromethoxy)-2-methoxyethane | HCID 77590 | — |
| Reactant | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Reactant | HCID 178526495 | HCID 178526495 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22147941 | HCID 22147941 | 46% |
Reaction Steps
To a solution of 3-iodo-5-nitro-1H-indazole (10.0 g, 34.6 mmol) in THF (50 ml) was added sodium bis(trimethylsilyl)amide (1M in THF, 48.4 mmol, 48.4 ml) and the solution stirred at room temperature for 20 minutes. 2-methoxyethoxymethyl chloride (4.9 g, 39.1 mmol, 4.5 ml) was added and the solution stirred at room temperature for 15 hours. The reaction was quenched with ammonium chloride (30 ml, saturated aqueous) and extracted into ethyl acetate (3×50 ml). The combined organic extracts were dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by flash column chromatography on silica gel (1:1 EtOAc:hexanes) to give the title compound as an orange solid (6.0 g). 1H NMR (400 MHz, CDCl3) δ 3.35 (3H, s), 3.50–3.52 (2H, m), 3.68–3.70 (2H, m), 5.86 (1H, s), 7.69 (1H, d), 8.38 (1H, d), 8.53 (1H, s). MS (ES+) m/e=378.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07041687B2 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-45e6f6e4960d4ace8d257b4bfe1b7418 |
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| Source note | uspto-grants-2006_05 |
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